Organic dye used in dye-sensitized solar cell

ABSTRACT

An organic dye used in a dye-sensitized solar cell is described, having general formula (1): 
       D-Sp1-Ch-Sp2-Acc-Y   (1) 
     wherein the groups D, Ch, Acc and Y are conjugate with each other, the group D is a donor group, the group Ch is a chromophore rendering low HOMO-LUMO gap or a polyaromatic chromophore, the group Acc is an acceptor group, the group Y is an anchoring group, and each of Sp1 and Sp2 represents a single bond or a spacer group allowing conjugation between the groups D and Ch or between the groups Ch and Acc.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional of an application Ser. No. 11/236,935,filed on Sep. 27, 2005. The entirety of the above-mentioned patentapplication is hereby incorporated by reference herein and made a partof this specification.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to solar cell materials. Moreparticularly, the present invention relates to an organic dye used in adye-sensitized solar cell.

2. Description of the Related Art

The demand for energy conservation triggered the search for alternaterenewable energy sources. A practical solution is the adoption oflight-harvesting biological concepts. This biomimetic strategy has beenrecently translated into technological advances such as solar cells.Although silicon-based semiconductors dominated solar cell applicationsfor decades, recent demonstration of dye-sensitized solar cells (DSSCs)based on nano-crystalline TiO₂ by Grätzel et al. (e.g., O'Regan, B.;Grätzel, M. Nature 1991, 353, 737) opened up the opportunity for organicand organometallic dyes in this area. A dye with excellentlight-absorbing capability in the red and near-IR region,photostability, and redox stability is attractive for the functioning ofDSSCs.

Coumarin-, indoline-, cyanine-, and hemicyanine-based dyes have beenused for the construction of DSSCs recently. However, the performancesof DSSCs based on these large molecules are usually insufficient. On theother hand, though polymers based on small chromophoric groups likebenzothiadiazole group have been employed in photovoltaic applications(e.g., van Duren, J. K. J.; Dhanabalan, A.; van Hal, P. A.; Janssen, R.A. J. Synth. Metals 2001, 121, 1587), small molecules containing suchsmall chromophoric groups are never exploited for DSSCs.

SUMMARY OF THE INVENTION

Accordingly, this invention provides an organic dye used in adye-sensitized solar cell, which is a small molecule containing achromophore rendering a low HOMO-LUMO gap or a polyaromatic chromophoreas a light-harvesting functional group.

The organic dye used in a dye-sensitized solar cell of this inventioncan be expressed by formula (1):

D-Sp1-Ch-Sp2-Acc-Y   (1)

wherein the groups D, Ch, Acc and Y are conjugate with each other, thegroup D is a donor group, the group Ch is a chromophore rendering lowHOMO-LUMO gap or a polyaromatic chromophore, the group Acc is anacceptor group, the group Y is an anchoring group, and each of Sp1 andSp2 represents a single bond or a spacer group allowing conjugationbetween the groups D and Ch or between the groups Ch and Acc.

By including a chromophore rendering low HOMO-LUMO gap or a polyaromaticchromophore in the dye molecule, the performance of the presentdye-sensitized solar cells can be improved dramatically when compared tothat fabricated from certain cyanine and hemicyanine dyes.

It is to be understood that both the foregoing general description andthe following detailed description are exemplary, and are intended toprovide further explanation of the invention as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the absorption spectra of the dyes S1-S4 recorded in THF inExamples 1-4 of this invention.

FIG. 2 shows the action spectra for the dyes S1-S4 in Examples 1-4.

FIG. 3 shows the absorption and emission spectra of the dyes 9, 12 and13 recorded in THF in Examples 5-9 of this invention.

FIG. 4 shows the absorption spectra of the dye 9 that is adsorbed onnano-crystalline TiO₂ and the action spectra for the DSSC constructedusing the dye 9.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

For the above organic dye expressed by formula (1), one example of thegroup Ch as a chromophore rendering low HOMO-LUMO gap is abenzo-[1,2,5]-thiadiazol-4,7-diyl or a benzo[1,2,5]selenadiazol-4,7-diylgroup as expressed by:

wherein X represents sulfur or selenium. This type of heteroaromaticgroup has a low-lying LUMO and is electron-deficient.

One example of the group Ch as a polyaromatic chromophore is a(poly)thienylfluorene group including one to three thienylfluorenesegments expressed by the following formula, or a derivative thereofobtained by substituting at least one H-atom thereon with a C₁-C₄ alkylgroup.

For example, the two H-atoms on position 9 of the fluorene group can besubstituted by ethyl groups to obtain the following group Ch. This typeof light-harvesting segment may have higher absorption coefficient.

Another example of the group Ch as a chromophore rendering low HOMO-LUMOgap is a group expressed by the following formula, wherein X representssulfur or selenium, and each of R1 and R2 represents hydrogen or a C₁-C₄alkyl group. This type of heteroaromatic group has a low-lying LUMO, andis electron-deficient.

Another example of the group Ch as a polyaromatic chromophore is acarbazolyl group expressed by the following formula, or a derivativethereof obtained by substituting at least one H-atom thereon with aC₁-C₄ alkyl group, wherein R3 represents hydrogen or a C₁-C₄ alkylgroup. This type of light-harvesting group may have higher extinctioncoefficient.

Another example of the group Ch as a polyaromatic chromophore is a fusedthienylthiophene-based group expressed by the following formula, or aderivative thereof obtained by substituting at least one H-atom thereonwith a C₁-C₄ alkyl group.

Another example of the group Ch as a polyaromatic chromophore is athiophene-based group expressed by the following formula, or aderivative thereof obtained by substituting at least one H-atom thereonwith a C₁-C₄ alkyl group, wherein n is equal to 2 or 3.

Another example of the group Ch as a polyaromatic chromophore is a groupexpressed by the following formula, or a derivative thereof obtained bysubstituting at least one H-atom thereon with a C₁-C₄ alkyl group.

The donor group D is, for example, a dialkylamino group or a diarylaminogroup, wherein the diarylamino group may contain at least one phenylgroup, 1-naphthyl group, 9-anthracenyl group or 1-pyrenyl group. Theacceptor group Acc is a 2-cyanoacryloxy or 2-cyanovinyl group, forexample. The anchoring group Y may be a carboxylic acid group that canbind with TiO₂ to anchor the dye molecule. Preferably, the acceptorgroup Acc and the anchoring group Y in combination include a2-cyanoacrylic acid group.

The symbol “Sp1” in formula (1) represents a single bond or a spacergroup allowing conjugation between the groups D and Ch. When Sp1represents a spacer group, examples of the spacer group include ap-phenylene group, a 2,5-thienylene group, the following group Sp1a andthe following group Sp1b, wherein n is equal to 2 or 3.

The symbol “Sp2” in formula (1) represents a single bond or a spacergroup allowing conjugation between the groups Ch and Acc. When Sp2represents a spacer group, examples of the spacer group include a2,5-thienylene group, a butadien-1,4-diyl group that may have a sidechain on the 3-carbon atom forming a five- or six-member ring with theacceptor group Acc as in formula (10) mentioned later, apyrimidine-2,5-diyl group, or a trans-vinylene-2,5-thiazolylene groupshown below.

The preferred combinations of the above-mentioned groups D, Ch, Acc andY, together with Sp1 and Sp2 each as a single bond or a spacer group,are expressed by the following formulae (2)-(13).

wherein Ar1 in formula (2) represents a p-phenylene group or a2,5-thienylene group, Ar2 in formulae (3) and (10)-( 13) represents1-naphthyl, 9-anthracenyl or 1-pyrenyl, each of R1 and R2 in formula(9), R3 in formula (12) and R4 and R5 in formula (13) representshydrogen or a C₁-C₄ alkyl group, X in formulae (2) and (4)-(9)represents sulfur or selenium, m in formula (3) is an integer of 1-3, nin formulae (5)-(7) and (10) is equal to 2 or 3, and each aprotic H-atomin each of formulae (2)-(13) can be substituted with a C₁-C₄ alkylgroup.

Some examples among the above dyes are tested for theirabsorption/emission spectra and evaluated for their photovoltaicperformances. These examples are given to further explain thisinvention, but are not intended to restrict the scope of the same.

EXAMPLES 1-4

In Examples 1-4, four dye compounds S1-S4 of general formula (2) arerespectively synthesized and investigated.

Example 1: dye S1, X=S, Ar=C₆H₄ (p-phenylene)

Example 2: dye S2, X=Se, Ar=C₆H₄

Example 3: dye S3: X=S, Ar=C₄H₂S (2,5-thienylene)

Example 4: dye S4: X=Se, Ar=C₄H₂S

In benzo(thia/selena)diazole-based fluorophores, the low-energyabsorption is predominantly charge transfer in nature, and the same istrue with the low-lying excited state also. This will ensure and enhancethe possibility of charge separation and migration in such systems. Thedyes were obtained in moderate yields in three steps as illustrated inScheme 1.

In the first step, the donor is attached to the core either by Stille orSuzuki coupling reactions. These reactions produced the disubstitutedside products as well. However monocapped compounds can be easilyseparated by column chromatography. In the next step, this bromo-exposedintermediate was reacted with(5-(1,3-dioxolan-2-yl)thiophen-2-yl)tributyl stannane under Stillecoupling conditions, and subsequent cleavage of the 1,3-dioxalaneprotecting group in aqueous acetic acid produced the free aldehydes.These aldehydes, on reaction with cyanoacetic acid in the presence ofammonium acetate catalyst in acetic acid, produced the required dyes.The dyes are dark red or black in the solid state and freely dissolve intetrahydrofuran (THF) to produce a red or violet solution.

TABLE 1 Electrooptical Parameters of the Dyes^(a) λ_(abs)/nm E_(1/2)(ox)E_(1/2)(red) HOMO, LUMO, Band Dye (ε × 10⁻³M⁻¹cm⁻¹) (ΔE_(p))/mV(ΔE_(p))/mV eV Ev gap, eV S1 491 (27.5), 388 581 (91) −1718 (90) 5.3813.260 2.121 (16.3), 309 (28.4) S2 502 (6.30), 351 556 (77) −1630 (96)5.356 3.338 2.018 (15.6) S3 541 (24.4), 398 322 (85) −1660 (106) 5.1223.256 1.866 (20.1), 312 (21.0) S4 544 (13.2), 363 263 (107) −1556 (138)5.063 3.290 1.773 (26.5) ^(a)Absorption and electrochemical data werecollected in tetrahydrofuran solutions. Scan rate, 100 mV/sec;electrolyte, (n-C₄H₉)₄NPF₆; ΔE_(p) is the separation between the anodicand cathodic peaks. Potentials are quoted with reference to the internalferrocene standard (E_(1/2) = +265 mV vs. Ag/AgNO₃).

The absorption spectra recorded for the THF solution of the dyes aredisplayed in FIG. 1. All the dyes exhibit three transitions and cover abroad range (250-700 nm) of spectra (FIG. 1 and Table 1). For thesimilar structural architecture, the benzoselenadiazole derivatives (S2and S4) display red-shifted absorption when compared to thebenzothiadiazole analogues (S1 and S3). However, the benzoselena-diazolederivatives possess less optical density for the CT transition. Anothereffect due to the linking aromatic segment was also noticed, i.e., thethiophene-linked compounds (S3 and S4) show bathochromic shift for thecharge-transfer band when compared to the phenylene-linked derivatives(S1 and S2).

The drop in the extinction coefficient of the CT absorption in thebenzoselena-diazole derivatives (S2 and S4) is more pronounced for thephenylene-conjugated derivative S2 (4.37 times when compared to S1) thanfor the thiophene-linked analogue S4 (1.85 times when compared to S3).These observations are attributed to the larger size and smallerelectronegativity of Se when compared to S. These factors will lead toless electron density on Se and thus diminished aromaticity forbenzoselenadiazole when compared to benzothiadiazole. Similarly, theincreased donor property and coplanar arrangement of thiophene with thecore substantially compensate the drop in transition probability for S4.

The dyes are redox stable, exhibiting both quasi-reversible oxidationand reduction couples. Dyes with good redox stability are required forsustaining dye-sensitized solar cells. Benzothiadiazole-basedderivatives containing triarylamines have been reported to undergofacile oxidation and reduction. Similarly, in the current derivatives,the oxidation and reduction also originate from the amino andbenzothiadiazole/benzoselenadiazole functionality, respectively.Thiophene linker slightly influences the redox potentials.Benzoselenadiazole derivatives display negative shift in oxidationpotentials and positive shift in the reduction potentials when comparedto the benzothiadiazole derivatives. This results in a substantialreduction in the band gap for the benzoselenadiazole derivatives whencompared to the benzothiadiazole analogues (see Table 1).

The dye-sensitized solar cells were constructed using these dyes as asensitizer for nano-crystalline anatase TiO₂. Typical solar cells, withan effective area of 0.25 cm², were fabricated with 0.05M I₂/0.5MLiI/0.5M tert-butyl pyridine in acetonitrile solution as an electrolyte.The device performance statistics under AM 1.5 illumination arecollected in Table 2. The incident to photon conversion efficiency dataat each wavelength are plotted for S1-S4 in FIG. 2. From the data, it isevident that dyes S1 and S2 exhibit impressive photovoltaicperformances. The open-circuit photovoltage and overall yield for thefour dyes lie in the order S1>S2>S3-S4.

TABLE 2 Performance Parameters of DSSCs Constructed Using the Dyes^(a)Dye V_(OC), mV J_(SC), mA cm⁻² ff η, % S1 546 10.44 0.66 3.77 S2 5248.35 0.67 2.91 S3 517 3.21 0.69 1.15 S4 474 3.57 0.66 1.11 N3 708 11.280.66 5.30 ^(a)Experiments were conducted using TiO₂ photoelectrodes withapproximately 14 μm thickness and 0.25 cm² working area on the FTO (7Ω/sq) substrates.

The difference in performance between the phenylene-conjugatedderivatives (S1 and S2) and the thiophene-linked analogues (S3 and S4)probably stems from the difference in the coplanarity of the aromaticsegment that bridges the donor and acceptor units. Molecular modeling(SPARTAN, PM3) studies reveal that the phenlylene derivatives (S1 andS2) possess a twisted non-planar geometry, which will decelerate therecombination of charges in the charge-separated state. Additionally, inthe phenylene derivatives (S1 and S2), the reorganization energyrequired for the decoupled twisted state may be more favorable whencompared to the thiophene analogues (S3 and S4).

Energy-minimized structure of S1:

Energy-minimized structure of S3:

Accordingly, the above-mentioned benzo(thia/selena)diazole-based dyescan be successfully adsorbed on nano-crystalline anatase TiO₂ particlesto form efficient dye sensitized solar cells. The performance of thesesmall-molecule-based, dye-sensitized solar cells is better than thatfabricated from certain cyanine and hemicyanine dyes (e.g., Yao, Q.-H.;Meng, F.-S.; Li, F.-Y.; Tian, H.; Huang, C.-H. J. Mater Chem. 2003, 13,1048). The approach is unique in that it uses an easily polarizable andelectron-deficient bridge between the push-pull chromophores, leading topush-pull-pull architecture that is different from that used previously,which contains a donor and an acceptor bridged through an aromatic oraliphatic linker.

EXAMPLES 5-9

In Examples 5-9, five dye compounds 9-13 of general formula (3) arerespectively synthesized and investigated. The thienylfluorene group informula (3) is an electron-rich group

Example 5: dye 9, n=1; Ar=1-naphthyl

Example 6: dye 10, n=1; Ar=9-anthracenyl

Example 7: dye 11, n=1; Ar=1-pyrenyl

Example 8: dye 12, n=2; Ar=1-naphthyl

Example 9: dye 13, n=3; Ar=1-naphthyl

The dyes were constructed by an iterative synthetic protocol illustratedin Scheme 2.

From the known compound,2-(7-bromo-9,9-diethyl-9H-fluoren-2-yl)thiophene (2), diarylaminesubstituted fluorenylthiophene derivatives (3-5) were obtained by theC—N coupling reactions involving Hartwig's catalyst and thecorresponding diarylamine. These thiophene derivatives were convertedinto their corresponding thiophenealdehydes (6-8) by lithiation withn-butyl lithium and subsequent quenching with dimethylformamide. Laterthe aldehydes 6-8 were converted to the dyes 9-11 by reaction withcyanoacetic acid in refluxing acetic acid in the presence of ammoniumacetate. In the another step, the stannylene precursor of the derivative3 prepared by treating the lithium derivative of the derivative 3 withtributyltin chloride in THF was used in the Stille reaction with thecompound 2 to produce the bis(thienylfluorene) conjugated analog of thederivative 3. This was then converted to the aldehyde which produced thedye 12 on treatment with cyanoacetic acid. One more similar iterativesequence starting with the bis(thienylfluorene) conjugated analog of thederivative 3 was executed to obtain the third generation dye 13. Thedyes are red colored and soluble in THF.

TABLE 3 Optical, redox and DSSCs performance parameters of the dyesλ_(abs), nm λ_(em), nm V_(OC), J_(SC), Dye (ε, M⁻¹W⁻¹) (Φ_(F), %) E_(ox)(ΔE_(p)), mV V mA/cm² ff η (%) 9 421 (52,900) 538 (0.28) 509 (82) 0.6512.47 0.65 5.23 10 421 (46,300) 536 (0.19) 451 (109) 0.57 7.59 0.67 2.8611 425 (54,500) 537 (0.33) 462 (66) 0.60 8.38 0.67 3.35 12 423 (95,500)512 (0.26) 447 (59), 613 (61) 0.61 9.83 0.65 3.89 13 423 (1,59,200) 472,504 (0.37) 437 (65), 569 (70) 0.61 9.81 0.64 3.80 N3 0.62 13.98 0.635.50

The absorption and emission spectra of the dyes recorded in THF solutionare displayed in FIG. 3 and the data are collected in Table 3. All thedyes exhibit a single prominent band probably the representing thesuperposition of π-π* and charge transfer transitions. The opticaldensity of this band increases rapidly on extending the conjugation byintroducing the additional thienylfluorene segments (FIG. 3). Thesecompounds are the first examples of DSSC active dyes to date to displaylarger absorption coefficients. Interestingly, the interaction betweenthe donor and acceptor gets minimized on increasing the conjugationlength of the bridge. This is reflected in the emission band position ofthe dyes 9, 12 and 13. Consequently, this slightly deters the magnitudeof charge separation for elongated derivatives 12 and 13.

The dyes can be reversibly oxidized at moderately high oxidationpotentials. The oxidation potentials are more positive than theferrocene/ferrocenium and I⁻/I⁻ ₃ redox couples. Oxidation higher thaniodine couple is necessary to forbid the backward electron transfer toelectrolyte solution and ensure forward electron injection into the TiO₂layer in the DSSC setup. The reversibility of the oxidation couple willbe beneficial for the stability of the DSSCs on long run.

The DSSCs fabricated, with effective area 0.25 cm², using these dyes aslight harvesting sensitizers, nano-crystalline anatase TiO₂ particles,and the electrolyte composed of 0.05M I₂/0.5M LiI/0.5Mtert-butylpyridine in acetonitrile solution showed impressivephoton-to-electron conversion. The device performance statistics underAM 1.5 illumination are listed in Table 3. Particularly the devicemanufactured with the dye 9 performed closely as the standard rutheniumdye N3. The action spectra and absorption spectra of the dye 9 adsorbedon TiO₂ is presented in FIG. 4. We believe that the dark currentminimization due to difficulty in the oxidation of dye 9 accounts forthe difference in performance among the dyes. Incidentally, theoxidation potential of 9 is slightly higher than other dyes.Additionally, energy minimized ground and excited state structures ofthe dye 9 and ground state structure of the dye 12 possesses twistedthienyl and fluorenyl segments. On the contrary, the excited statestructure of the dye 12 is predominantly coplanar in nature. A coplanarexcited state structure may enhance the effective conjugation andfacilitate the charge recombination processes. Consequently, the excitedstate dipole moment of 9 is double than that of the ground stategeometry. However the conjugated dyes (12 and 13) do not show any changein the ground and excited state dipole moments.

Accordingly, Examples 5-9 investigate a series of dyes featuringthienylfluorene conjugation, diarylamine donors and 2-cyanoacrylic acidacceptors. Despite the lower wavelength absorption, the DSSC performanceachieved for a dye nearing to that of N3 is intriguing.

In summary, this invention provides a new class of dyes featuringdonor-acceptor architecture that incorporates a chromophore renderinglow HOMO-LUMO gap or a polyaromatic chromophore. They can besuccessfully adsorbed on nano-crystalline anatase TiO₂ particles to makeefficient DSSCs. The performance of these small-molecule-based,dye-sensitized solar cells is better than that fabricated from certaincyanine and hemicyanine dyes. This design opens up the possibility ofpreparing new dye molecules for DSSCs utilizing low-band-gap buildingblocks.

It will be apparent to those skilled in the art that variousmodifications and variations can be made to this invention withoutdeparting from the scope or spirit of this invention. Hence, it isintended that this invention covers its modifications and variationsprovided they fall within the scopes of the claims and theirequivalents.

1. An organic dye used in a dye-sensitized solar cell, expressed by formula (1): D-Sp1-Ch-Sp2-Acc-Y   (1) wherein the groups D, Ch, Acc and Y are conjugate with each other, the group D is a donor group, the group Acc is an acceptor group, the group Y is an anchoring group, each of Sp1 and Sp2 represents a single bond or a spacer group allowing conjugation between the groups D and Ch or between the groups Ch and Acc, and the group Ch is a (poly)thienylfluorene group including one to three thienylfluorene groups expressed by the following formula:

or a derivative thereof obtained by substituting at least one H-atom thereon with a C₁-C₄ alkyl group.
 2. The organic dye of claim 1, wherein the group Ch is a (poly)thienylfluorene group expressed by the following formula:


3. The organic dye of claim 1, wherein the donor group D comprises a dialkylamino group or a diarylamino group.
 4. The organic dye of claim 3, wherein the diarylamino group contains at least one phenyl group, 1-naphthyl group, 9-anthracenyl group or 1-pyrenyl group.
 5. The organic dye of claim 1, wherein the acceptor group Acc comprises a 2-cyanovinyl group.
 6. The organic dye of claim 1, wherein the anchoring group Y comprises a carboxylic acid group.
 7. The organic dye of claim 1, wherein the acceptor group Acc and the anchoring group Y in combination include a 2-cyanoacrylic acid group.
 8. The organic dye of claim 1, wherein Sp1 represents a p-phenylene group, a 2,5-thienylene group, the following group Sp1a or the following group Sp1b:

wherein n is equal to 2 or
 3. 9. The organic dye of claim 1, wherein Sp2 represents a 2,5-thienylene group, a butadien-1,4-diyl group that optionally has a side chain on the 3-carbon atom forming a five- or six-member ring with the acceptor group Acc, a pyrimidine-2,5-diyl group, or a trans-vinylene-2,5-thiazolylene group.
 10. The organic dye of claim 2, having the following formula:

wherein Ar2 represents 1-naphthyl, 9-anthracenyl or 1-pyrenyl, and each aprotic H-atom can be substituted with a C₁-C₄ alkyl group. 